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HRID 35518作成日:2026年10月24日

2-Amino-5-methylpyridine → 6-Methyl-2-[4-(trifluoromethyl)phenyl]imidazo[1,2-a]pyridine

https://huagongshe.com/ja/reaction/35518

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-5-methylpyridineHCID 15348—
反応物2-Bromo-4'-(trifluoromethyl)acetophenoneHCID 321979—
反応物Sodium BicarbonateHCID 516892—
溶媒EthanolHCID 702—
生成物6-Methyl-2-[4-(trifluoromethyl)phenyl]imidazo[1,2-a]pyridineHCID 2813810—

反応手順

24 g (0.077 mole) of 1-bromo-2-(4-trifluoromethylphenyl)-2-ethanone, 8.4 g (0.077 mole) of 2-amino-5-methylpyridine and 13 g of sodium bicarbonate are mixed in 210 ml of 95% strength ethanol, and this suspension is heated under reflux until the evolution of gas has ceased. The solvent is then evaporated off under reduced pressure and the evaporation residue is taken up with water and dichloromethane. The organic phase is decanted and dried over magnesium sulphate, and the solvent is removed by evaporation under reduced pressure. The residue is purified by column chromatography.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04767755
出典データセットuspto-grants-1988_08
ORD IDord-a4f089c2a14f4280abf7024273451486
出典メモuspto-grants-1988_08